肠道微生物群、代谢物与 "肌肉疏松症 "之间的因果关系:孟德尔随机化研究。

Xiangyu Zhang, Guang Yang, Shide Jiang, Bingzhou Ji, Wenqing Xie, Hengzhen Li, Jianfeng Sun, Yusheng Li
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引用次数: 0

摘要

背景:在老年人群中经常观察到肠道微生物群失衡和肌肉疏松症。肠道微生物群及其代谢产物被认为是导致肌少症风险增加的风险因素,但这些关联是否是因果关系仍不清楚:我们以大规模全基因组关联研究中的 SNPs 为工具变量,采用关联不平衡得分回归和双样本孟德尔随机方法,研究肠道微生物群及其代谢物与肌肉疏松症之间的因果关系。在进行了MR分析后,又进行了敏感性分析,以加强所得结果的稳健性和可信度:磁共振分析得出了令人信服的证据,证明了基因预测的肠道微生物群和代谢物与肌肉疏松症风险之间的相关性。研究发现,卟啉单胞菌科(Porphyromonadaceae)、Rikenellaceae、Terrisporobacter 和 Victivallis 的丰度与 WP 相关。我们的研究还发现,12 种肠道细菌与 ALM 相关,链球菌科、肠杆菌科、副链球菌科、反刍球菌科 UCG009 和 Sutterella 与 GS 相关。具体来说,我们发现了 21 种肠道微生物群衍生代谢物可能与肌少症风险有关:我们的研究利用双样本磁共振方法,阐明了肠道微生物群、肠道微生物群衍生代谢物与肌少症发生之间的因果关系。这些发现表明,肠道微生物群和代谢物可能是导致肌肉疏松症的潜在风险因素,并有望成为新的治疗重点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Causal Relationship Between Gut Microbiota, Metabolites, and Sarcopenia: A Mendelian Randomization Study.

Background: Gut microbiota imbalance and sarcopenia are frequently observed in older adults. Gut microbiota and their metabolites are considered risk factors contributing to the heightened risk of sarcopenia, but whether these associations are causal remains unclear.

Methods: We conducted linkage disequilibrium score regression and 2-sample Mendelian randomization (MR) methods with single-nucleotide polymorphisms sourced from large-scale genome-wide association studies as instrumental variables to examine the causal associations linking gut microbiota with their metabolites to the sarcopenia. Following the MR analysis, subsequent sensitivity analyses were conducted to reinforce the robustness and credibility of the obtained results.

Results: MR analysis yielded compelling evidence demonstrating the correlation between genetically predicted gut microbiota and metabolites and the risk of sarcopenia. The abundance of Porphyromonadaceae, Rikenellaceae, Terrisporobacter, and Victivallis was found to be associated with walking pace. Our study also found suggestive associations of 12 intestinal bacteria with appendicular lean mass, and of Streptococcaceae, Intestinibacter, Paraprevotella, Ruminococcaceae UCG009, and Sutterella with grip strength. Specifically, we identified 21 gut microbiota-derived metabolites that may be associated with the risk of sarcopenia.

Conclusions: Utilizing a 2-sample MR approach, our study elucidates the causal interplay among gut microbiota, gut microbiota-derived metabolites, and the occurrence of sarcopenia. These findings suggest that gut microbiota and metabolites may represent a potential underlying risk factor for sarcopenia, and offer the promise of novel therapeutic focal points.

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